By individually targeting lncRNAs for removal, scientists can see what the effect is on cell function. "This survey of ...

It’s been a year since the gene-editing treatment Casgevy was approved for sickle cell disease and a related blood disorder.

CRISPR Therapeutics ( CRSP -5.91%) made a name for itself by pioneering advanced gene therapies made with technologies that didn't exist a generation ago. Now, its challenge is to build on its prior ...

Using CRISPR, the popular gene-editing tool, scientists bumped up the fruit’s sugar content by 30 percent without sacrificing ...

Researchers used base and prime editing to uncover new EGFR gene mutations that affect cancer progression and drug resistance ...

Harvard researchers pioneered a method called HACE for targeted gene mutations, advancing genetic research potential.

Gene mutations have consequences both good and bad—from resistance to conditions like diabetes to susceptibility to certain ...

Researchers at ETH Zurich combined two CRISPR-Cas methods to decipher how mutations in a cell’s genome affect its function.

In recent years, scientists have created a range of new methods based on CRISPR-Cas technology for precisely editing the ...

To separate AI hype from reality in medicine, a doctor and author of a book on generative AI’s future in medicine suggests asking three simple questions.

Genes contain instructions for making proteins, and a central dogma of biology is that this information flows from DNA to RNA to proteins. But only two percent of the human genome actually encodes ...

An RNA-editing gene therapy has been developed that switches off the key driver of common eye conditions affecting diabetics ...